HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → 4-(4'-Methoxyanilino)-7-trifluoromethylquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | 4-Chloro-7-(trifluoromethyl)quinazoline | HCID 12806742 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4'-Methoxyanilino)-7-trifluoromethylquinazoline | HCID 12806775 | 79.2% |
Reaction Steps
5 ml of ethanol were added to a mixture of 2.3 g of 4-chloro-7-trifluoromethylquinazoline and 1.4 g of p-anisidine. The resulting mixture was heated to dissolve the solids, whereupon the solution solidified immediately. After cooling, the resulting crystals were collected by filtration and washed with, in turn, ethanol, dilute aqueous sodium hydroxide and water. The resulting crystals were recrystallized from ethanol, to give 2.5 g (yield 78%) of the desired Compound No. 51 in the form of colourless needles melting at 190°-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04322420 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-d53d93b40fc149e7a6862c357427ee91 |
| Source note | uspto-grants-1982_03 |